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61.
We present an analysis with improved sensitivity to the light charged Higgs (mH+ < mt-mbm_{H^{+}} < m_{t}-m_{b}) searches in the top quark decays tbH +b(τ + ν τ )+c.c. in the t[`(t)]t\bar{t} and single t/[`(t)]t/\bar{t} production processes at the LHC. In the Minimal Supersymmetric Standard Model (MSSM), one anticipates the branching ratio B (H+ ?t+nt) @ 1{\mathcal{B}} (H^{+} \to\tau^{+}\nu_{\tau})\simeq1 over almost the entire allowed tanb\tan\beta range. Noting that the τ + arising from the decay H +τ + ν τ are predominantly right-polarized, as opposed to the τ + from the dominant background W +τ + ν τ , which are left-polarized, a number of H +/W +τ + ν τ discriminators have been proposed and studied in the literature. We consider hadronic decays of the τ ±, concentrating on the dominant one-prong decay channel τ ±ρ ± ν τ . The energy and p T of the charged prongs normalised to the corresponding quantities of the ρ ± are convenient variables which serve as τ ± polariser. We use the distributions in these variables and several other kinematic quantities to train a boosted decision tree (BDT). Using the BDT classifier, and a variant of it called BDTD, which makes use of decorrelated variables, we have calculated the BDT(D)-response functions to estimate the signal efficiency vs. the rejection of the background. We argue that this chain of analysis has a high sensitivity to light charged Higgs searches up to a mass of 150 GeV in the decays tbH + (and charge conjugate) at the LHC. For the case of single top production, we also study the transverse mass of the system determined using Lagrange multipliers.  相似文献   
62.
Electromagnetically induced absorption (EIA) was observed for the first time on a sample of 85Rb in a magneto-optical trap using low intensity cw copropagating pump and probe optical fields. Narrow resonances revealing the dependence of the ground-state Zeeman sublevels energy structure on the quadrupolar magnetic field and the trapping optical field intensity at different trap positions, were observed. Coherence resonances as narrow as 30 kHz were obtained under low trapping field intensities. The use of EIA spectroscopy for the magnetic field mapping of cold atomic samples is illustrated.  相似文献   
63.
The efficiency of antioxidants to inhibit the oxidation of lipid‐based emulsions depends on several factors including their nature and their concentration at the reaction site. Here, we have analyzed the effects of acidity and of surfactant concentration on the distribution and efficiency of the vitamin E analog Trolox (TR) in stripped olive oil‐in‐water emulsions stabilized with Tween 20. The distribution was assessed in the intact emulsions by employing a kinetic method that exploits the reaction between the hydrophobic 4‐hexadecylbenzenediazonium ions and TR. Kinetic results are interpreted on the grounds of the pseudophase model. The effects of TR on the oxidative stability of the emulsion were determined at different pH values by monitoring the formation of conjugated dienes over time. The results show that the efficiency of TR increases upon increasing pH even though its concentration in the interfacial region decreases.  相似文献   
64.
We present the first data on photon-photon annihilation into hadrons for CM energies > 1 GeV obtained with the detector PLUTO at the e+e? storage ring PETRA. Cross sections are extracted using an inelastic eγ scattering formalism. The results are compared to expectations from Regge-like models.  相似文献   
65.
    
Determining the association constants of radicals to biomimetic systems is not a simple task because of the inherent experimental difficulties associated to their “in‐situ” generation together with their high chemical instability, requiring the use of radical trapping agents in combination with, for example, magnetic (eg, EPR) and/or time‐resolved techniques (eg, frequency comb spectroscopy) to indentify and quantify them. Here, we have exploited the unique electrochemical properties of arenediazonium ions, ArN2+, to estimate the association constant of the electrochemically generated aryl radicals derived from benzenediazonium ions, BD, with sodium dodecyl sulfate (SDS) micelles. When ArN2+ are reduced on an Hg electrode, they acquire an electron yielding the corresponding arenediazenyl radical, ArN2, which undergoes further decomposition to produce the aryl radical, Ar. BD partitions between the aqueous and micellar pseudophases, and, upon increasing [SDS], peak currents decrease and the peak potentials are shifted. Results indicate that the association constant of the aryl radical to SDS micelles is 3 times higher than that of the parent substrate as a consequence of its higher hydrophobicity compared with that of the parent molecule. The method is feasible because of the large number of arenediazonium ions that can be prepared and because it does not depend on the reactivity of the electrochemically generated radical.  相似文献   
66.
    
With the view to altering the lipophilicity and electron accepting ability of the tetraphenyl‐carbo‐benzene scaffold, peripheral fluorination of the C18 ring through aromatic linkers was envisaged from the C18Ph6 and otBu2C18Ph4 references, by replacement of two Ph substituents with two p‐CF3‐C6H4 counterparts (FTol). The synthesis relied on a [8+10] macrocyclization involving a common bis(trifluorotolyl)‐tetraynedione, followed by reductive aromatization of the resulting [6]pericyclynediols. While pFTol2C18Ph4 proved to be hardly tractable due to an extremely low solubility, pFTol2otBu2C18Ph2 could be extensively studied by X‐ray crystallography, NMR and UV/Vis spectroscopy, voltammetry, STM imaging of monolayers, and AFM imaging of binary films with P3HT or PC71BM fabricated by spin‐coating for organic photovoltaic cells and J?V curve measurement thereof. The electronic and polarity properties are correlated with moderate but consistent electron‐withdrawing effects of the CF3 groups, in agreement with the DFT‐calculated frontier orbitals and multipole moments. The results provide guidelines for optimization of fluorinated carbo‐benzene targets.  相似文献   
67.
    
In this work, we evaluated the conformational effect promoted by the isosteric exchange of sulfur by selenium in the heteroaromatic ring of new N-acylhydrazone (NAH) derivatives (3–8, 13, 14), analogues of the cardioactive compounds LASSBio-294 (1) and LASSBio-785 (2). NMR spectra analysis demonstrated a chemical shift variation of the iminic Csp2 of NAH S/Se-isosters, suggesting a stronger intramolecular chalcogen interaction for Se-derivatives. To investigate the pharmacological profile of these compounds at the adenosine A2A receptor (A2AR), we performed a previously validated functional binding assay. As expected for bioisosteres, the isosteric-S/Se replacement affected neither the affinity nor the intrinsic efficacy of our NAH derivatives (1–8). However, the N-methylated compounds (2, 6–8) presented a weak partial agonist profile at A2AR, contrary to the non-methylated counterparts (1, 3–5), which appeared as weak inverse agonists. Additionally, retroisosterism between aromatic rings of NAH on S/Se-isosters mimicked the effect of the N-methylation on intrinsic efficacy at A2AR, while meta-substitution in the phenyl ring of the acyl moiety did not. This study showed that the conformational effect of NAH-N-methylation and aromatic rings retroisosterism changed the intrinsic efficacy on A2AR, indicating the S/Se-chalcogen effect to drive the conformational behavior of this series of NAH.  相似文献   
68.
The chiral GC separation of 2-alkyl-2-keto-gamma-butyrolactone derivatives and their alcohol analogs using 2,3-di-O-methyl-6-O-tert.-butyldimethylsilyl-beta-cyclodextrin (DIMETBCD) as chiral selector was discussed. The results, supported by the ketone preliminary molecular modelling calculations, suggest that the chiral recognition for DIMETBCD depends more on the geometry than on the polarity of the alkyl substituents on the butyrolactones. Hydrogen bonds and alkyl group steric effects should be an important function of the alcohol chiral recognition for DIMETBCD. Comparison of the retention times of the alcohol derivatives, in achiral and chiral stationary phases, suggests a specific structural effect for the cyclodextrin selctor.  相似文献   
69.
The phenolic potential of Tannat, Cabernet-Sauvignon and Merlot grapes was evaluated in 2001 and 2002 and its correspondence with the colour and composition of the respective wines was established. Three vineyards of each variety, situated in the south of Uruguay were considered. Two samples of each vineyard were taken at the moment of the harvest. Phenolic richness, extractable anthocyanins contents and total potential in anthocyanins of the grapes were estimated. Two fermentations on skins were carried out for each vineyard using 50 kg of grape in each one. The anthocyanic and total polyphenols contents of the musts were analysed every 24 h, and skins extractions were carried out in parallel in the laboratory. The duration of the maceration for each variety was decided in function of the analytical results in the grapes, musts and skins extractions. Wines were analysed 2 months after the alcoholic fermentation, determining its phenolic composition and colour. Tannat grapes presented anthocyanic and total polyphenols contents significantly higher in both years. Therefore, wines from this variety presented colour intensity and phenolic contents statistically higher than Cabernet-Sauvignon and Merlot. The correlations between the phenolic contents of the grapes, skins, musts and wines were very significant. Colour intensity and phenolic contents of the wines were highly correlated with the total polyphenols of the grapes and with anthocyanins of the grapes, skins, musts and wines. The estimate of the phenolic potential of the grapes and the extractability of the pigments allows to manage more adequately the fermentation on skins and is an interesting tool to predict the colour and the composition of the wines.  相似文献   
70.
A series of ω-carboalkenyl pyrazole derivatives have been synthesized as potential thromboxane-synthetase inhibitors considering the close bioisosteric relationship between the pyrazole ring and other heteroaromatic carboalkenyl compounds exhibiting inhibitory activity. (E)-7-(1-Phenylpyrazol-4-yl)hept-2-enoic acid (4b) were prepared in 28% overall yield from its minor bis-homologue, (E)-5-(1-phenylpyrazol-4-yl)pent-2-enoic acid (4a) , obtained from 4-formyl-1-phenylpyrazole (6) in 17% overall yield. Compounds 4a, 4b, 7, 8 and 13 were screened for their ability to inhibit the in vitro rabbit blood platelet aggregation induced by collagen using the Born test. Among the active compounds 4a exhibited an important inhibition at 1 μM concentration.  相似文献   
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